Company Profile
High-Quality APIs
Global Standards
Vedura delivers high-quality Active Pharmaceutical Ingredients (APIs) sourced from WHO-GMP, EU GMP, and USFDA-approved manufacturing facilities worldwide.
We specialize in customized API solutions, offering the flexibility to support both small-batch requirements and large-scale commercial production—while consistently adhering to the highest global regulatory standards.
Our comprehensive regulatory support ensures seamless integration into your pharmaceutical processes, including DMF filings, technical packages, and stability studies.
"At Vedura, quality, transparency, and customer-centricity form our foundation."
Accomplished pharmaceutical professional with over two decades of experience in API Sales and Business Development across diverse global markets.
Proven expertise in Bulk Drugs marketing, out-licensing, contract manufacturing, and strategic pricing across key regions.
Demonstrated ability to manage and grow portfolios spanning APIs, intermediates, nutraceutical bulk drugs, and peptides—across both niche and high-volume commoditized segments.
B.E (Chemical Engineering) from NIT Rourkela and MBA with specialization in International Business. Also holds Diploma in Pharmacy.
Expertise
Our Core Services
By combining sourcing expertise, market intelligence, and regulatory proficiency, Vedura delivers a seamless, end-to-end solution—reducing time-to-market and ensuring compliance.
Sourcing Excellence
Strategic identification and qualification of suppliers aligned with specific product and regulatory requirements.
- Supplier Assessment
- Negotiation Levers
- Sampling & Evaluation
- Regulatory Screening
Global Marketing
Development of international markets and customer networks for Indian manufacturers with credible partners.
- Market Access Strategy
- Indian Principal Alignment
- Product Registration
- Regulatory Frameworks
Regulatory Support
Streamlining product registration and ensuring smooth market access across global regulated and semi-regulated geographies.
- DMF (CEP, US-DMF, CADIFA)
- Technical Packages & Dossiers
- Stability Study Coordination
- Pharmacopeial Compliance
Contact
Start your
Inquiry
Looking for a specific molecule or high-volume sourcing? Reach out to us and our team will get back to you within 24 hours.
harpreet@vedurapharma.com
Phone
+91 96876 30061